HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1788963Generated: October 25, 2026
Nitrobenzene → 1-Ethyl-5-(2-thenoyl)oxindole
https://huagongshe.com/reaction/1788963
Participants
| Role | Name | HCID | Charge |
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| Reactant | Nitrobenzene | HCID 7416 | — |
| Reactant | N-Ethyloxindole | HCID 66135 | — |
| Reactant | 2-Thiophenecarbonyl chloride | HCID 78928 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-Ethyl-5-(2-thenoyl)oxindole | HCID 13770528 | 47.7% |
Reaction Steps
To a mixture of 27.3 g. (19.9 mmoles) of 2-thenoyl chloride, 30 ml. of nitrobenzene and 32.95 g. of aluminum chloride was gradually added 10 g. (62 mmoles) of 1-ethyloxindole, and the resulting reaction mixture heated at 100° C. for 75 minutes. The reaction was cooled to room temperature and poured into 2 l. of ice and water. The product was extracted with methylene chloride and the dried extract concentrated to dryness, 11.05 g. The product was recrystallized from methylene chloride-hexane, 8.03 g. (47.7% yield)m, m.p. 158°-160° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04686224 |
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| Source dataset | uspto-grants-1987_08 |
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| ORD ID | ord-0f9f5c833f7c431ea73c55a1b90f4562 |
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| Source note | uspto-grants-1987_08 |
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